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Improving HIV-2 Detection by a Combination of Serological and Nucleic Acid Amplification Test Assays

机译:结合血清学和核酸扩增测试方法改善HIV-2检测

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The ability to detect HIV-2 and to discriminate between HIV-1 and HIV-2 infections was evaluated in 46 serum samples from Guinea-Bissau (GB) and Guinea-Conakry (GC) using serological tests and commercial (HIV-1) and in-house (HIV-2) real-time PCR assays. Samples were first identified as HIV-2 positive by Genie I/II assay in GB and GC. HIV positivity was detected in 44 of 46 samples by all screening and confirmatory assays. A diagnostic strategy based on Inno-LIA and HIV-1/2 RNA detection assays allowed accurate discrimination between HIV-1 and HIV-2 in 84% of single infections and confirmed 32% of double infections. In samples with double reactivity in the Inno-LIA test and no detection of both genomes, cross-reactivity likely hampered the identification of true double infections. In conclusion, the implementation of a diagnostic strategy, based on multiple specific serological tests and highly sensitive quantitative PCR assays, is recommended to ensure accurate HIV-2 diagnosis and appropriate therapy for individuals from areas in which the virus is endemic.
机译:使用血清学检测和商业检测(HIV-1)对来自几内亚比绍(GB)和几内亚-科纳克里(GC)的46个血清样本中的HIV-2进行检测并区分HIV-1和HIV-2感染的能力。内部(HIV-2)实时PCR分析。首先通过GB和GC中的Genie I / II分析将样品鉴定为HIV-2阳性。通过所有筛选和确证分析,在46个样本中的44个样本中检测到HIV阳性。基于Inno-LIA和HIV-1 / 2 RNA检测方法的诊断策略可准确区分84%的单次感染的HIV-1和HIV-2和32%的双重感染。在Inno-LIA测试中具有双重反应性且未检测到两个基因组的样品中,交叉反应性可能会阻碍真正双重感染的鉴定。总之,建议基于多种特定的血清学检测和高度灵敏的定量PCR检测方法实施诊断策略,以确保对HIV-2流行地区的个体进行准确的HIV-2诊断和适当的治疗。

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